Published December 31, 2000 | Version v1
Taxonomic treatment Open

Bodo saliens Larsen and Patterson 1990

Description

Bodo saliens Larsen and Patterson, 1990

(fi gures 1j, 2p, q)

Description. Cell usually elongate elliptical and somewhat inflexible, 4-10 Mm long (mostly 6-9 Mm), 2-5 Mm wide. Two fl agella unequal in length emerge subapically from a shallow pocket. The anterior fl agellum appears inactive, is as long as or slightly shorter than the cell and is held forwards with a single anterior curve held perpendicular to the substratum. The acronematic posterior fl agellum is typically directed straight behind the cell and is about 2.2-3.5 times the cell length. Cells swim in rapid darts in straight lines. Frequently observed. Description based on observations of 21 cells.

Remarks. This species has been found in North Atlantic, subtropical and tropical Australia, Brazil, Arctic Canada, Denmark, West Greenland, Hawaii, Gulf of Finland and Panama, and previously reported size ranges are 5-15 Mm (Larsen and Patterson, 1990; Vørs, 1992a, 1992b, 1993a; Patterson et al., 1993; Ekebom et al., 1996; Patterson and Simpson, 1996; Tong et al., 1998). Generally, our observations are in accordance with those of previous observers. Bodo saliens is distinguished from other species of the genus Bodo by its rapid darting movement and the posterior fl agellum which is directed in a straight line. This species is similar in shape to B. curvi ®lus Griessmann, 1913, but it is distinguished because B. curvi ®lus has a paddling anterior fl agellum which is curved along its entire length.

Hemistasia phaeocysticola (Scherffel, 1900) Elbrächter et al., 1996 (fi gures 1k, 4a -e)

Description. Cell outline pyriform, about 13-15 Mm long, metabolic, with a fl exible apical papillum and with an indistinct spiral groove. Two fl agella insert subapically in a pocket, are unequal in length and wrap around the body during feeding. The posterior fl agellum is slightly longer than the anterior fl agellum and the cell. During swimming cells rotate. The cells often contain one large food vacuole up to 6 Mm in the posterior part of the cell. Observed eating the cytoplasm of diatoms. The nucleus was not seen. Rarely observed.

Remarks. According to Elbrächter et al. (1996), this species is identical with Hemistasia klebsii Griessmann, 1913 and Pronoctiluca phaeocysticola (Scherffel, 1900) Pavillard, 1922. They observed this species inside the shells of diatoms, dinoflagellates and copepods, and in cultures the species attacked diatoms, dinoflagellates and prymnesiophytes. This species was found in marine sites by Scherffel (1900), Griessmann (1913), Elbrächter et al. (1996) and Tong et al. (1998). Previous reported cell lengths range from 10 to 25 Mm. The genus Hemistasia resembles Entomosigma, Rhynchobodo and Cryptaulax. The latter two genera have recently been synonymized (Bernard et al., 1999). Hemistasia can be distinguished from Rhynchobodo by its anterior papillum. Hemistasia may be the same as the genus Entomosigma Schiller, 1925 (Patterson, 1994). Figure 3 of Elbrächter et al. (1996) is similar to fi gure 21 (I -II) of H. klebsii by Griessmann (1913) and the fi gures of Entomosigma peridinioides Schiller, 1925, and fi gures 5, 6 of Elbrächter et al. (1996) are also similar to the fi gure 3 of C. marina of Throndsen (1969). Cryptaulax marina sensu Throndsen, 1969 is believed to be H. phaeocysticola (Bernard et al., 1999).

Notes

Published as part of Lee, Won Je & Patterson, David J., 2000, Heterotrophic flagellates (Protista) from marine sediments of Botany Bay, Australia, pp. 483-562 in Journal of Natural History 34 on page 492

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Linked records

Additional details

Biodiversity

Family
Bodonidae
Genus
Bodo
Kingdom
Protozoa
Order
Bodonida
Phylum
Euglenozoa
Scientific name authorship
Larsen and Patterson
Species
saliens
Taxon rank
species
Taxonomic concept label
Bodo saliens and, 1990 sec. Lee & Patterson, 2000

References

  • LARSEN, J. and PATTERSON, D. J., 1990, Some ¯ agellates (Protista) from tropical marine sediments, Journal of Natural History, 24, 801 ± 937.
  • PATTERSON, D. J., NYGAARD, K., STEINBERG, G. and TURLEY, C., 1993, Heterotrophic ¯ agellates and other protists associated with oceanic detritus throughout the water column in the mid North Atlantic, Journal of the Marine Biological Association of the United Kingdom, 73, 67 ± 95.
  • EKEBOM, J., PATTERSON, D. J. and VORS, N., 1996, Heterotrophic ¯ agellates from coral reef sediments (Great Barrier Reef, Australia), Archiv fuEr Protistenkunde, 146, 251 ± 272.
  • PATTERSON, D. J. and SIMPSON, A. G. B., 1996, Heterotrophic ¯ agellates from coastal marine and hypersaline sediments in Western Australia, European Journal of Protistology, 32, 423 ± 448.
  • TONG, S. M., NYGAARD, K., BERNARD, C., VORS, N. and PATTERSON, D. J., 1998, Heterotrophic ¯ agellates from the water column in Port Jackson, Sydney, Australia, European Journal of Protistology, 34, 162 ± 194.
  • GRIESSMANN, K., 1913, U E ber marine Flagellaten, Archiv fuEr Protistenkunde, 32 (year 1914), 1 ± 78.
  • BERNARD, C., SIMPSON, A. G. B. and PATTERSON, D. J., 1999, Some free-living ¯ agellates from anoxic sediments, Ophelia, (in press).
  • PATTERSON, D. J., 1994, Protozoa: evolution and systematics, in K. Hausmann and N. HuElsmann (eds) Progress in Protozoology (Stuttgart), pp. 1 ± 14.
  • THRONDSEN, J., 1969, Flagellates of Norwegian coastal waters, Nytt Magasin for Botanik, 16, 161 ± 216.